The association of APOE genotype and cognitive decline in interaction with risk factors in a 65-69 year old community sample

BMC Geriatr. 2008 Jul 14:8:14. doi: 10.1186/1471-2318-8-14.

Abstract

Background: While the evidence of an association between the apolipoprotein E (APOE) *E4 allele and Alzheimer's disease is very strong, the effect of the *E4 allele on cognitive decline in the general population is more equivocal. A cross-sectional study on the lifespan effects of the *E4 allele 1 failed to find any effect of the *E4 allele on cognitive performance at ages 20-24, 40-44 or 60-64 years.

Methods: In this four year follow-up study, we reexamine the effect of *E4 in the sample of 2,021 individuals, now aged 65-69 years.

Results: Performance on the Mini-Mental State Examination (MMSE) was significantly poorer for *E4 homozygotes than heterozygotes or non-carriers. The effects of the *E4 genotype on cognitive decline over four years were found on the MMSE and Symbol-Digit Modalities test but only when controlling for risk factors such as head injury and education. Analyses were repeated with the exclusion of participants diagnosed with a mild cognitive disorder, with little change.

Conclusion: It is possible that *E4 carriers become vulnerable to greater cognitive decline in the presence of other risk factors at 65-69 years of age.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / genetics
  • Apolipoproteins E / genetics*
  • Australia
  • Cognition Disorders / diagnosis
  • Cognition Disorders / genetics*
  • Cross-Sectional Studies
  • Female
  • Follow-Up Studies
  • Genotype
  • Geriatric Assessment / methods*
  • Heterozygote
  • Humans
  • Intelligence Tests
  • Male
  • Middle Aged
  • Risk Factors

Substances

  • Apolipoproteins E